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Pregnant women undergoing cesarean will be the participants, half will be given paracetamol and half will be given diclofenac and pain measurement will be done post operatively.

Study of comparison Of pain relief profile between paracetamol and diclofenac suppository in post cesarean women - Nil

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
CTRI
Registry ID
CTRI/2026/05/110324
Enrollment
140
Registered
2026-05-11
Start date
Unknown
Completion date
Unknown
Last updated
2026-06-01

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Health Condition 1: O80- Encounter for full-term uncomplicated delivery

Interventions

Intervention1: diclofenac: 100 mg rectal suppository within 30 mins of skin closure 1 stat dose Per rectal Observation for 24 hours Control Intervention1: paracetamol: Dose 1 g intravenous infusion

Sponsors

National capital region institute of medical sciences
Lead Sponsor

Eligibility

Inclusion criteria

Inclusion criteria: pregnant women single live intrauterine pregnancy those giving consent

Exclusion criteria

Exclusion criteria: allergic to paracetamol / diclofenac complicated pregnancy derranged liver and kidney function tests those refusing consent

Design outcomes

Primary

MeasureTime frame
pain relief profileTimepoint: 24 hours—

Secondary

MeasureTime frame
ambulation time Timepoint: 24 hours;Unassisted breastfeeding durationTimepoint: 24 hours;side effectsTimepoint: 24 hours—

Countries

India

Contacts

Public ContactDr Aditi Bansal

Ncrims

dranitasingh1964@gmail.com8630084744

Outcome results

None listed

Source: CTRI (via WHO ICTRP) · Data processed: Jun 11, 2026